ARTICLE IN PRESS. Journal of Fluency Disorders xxx (2010) xxx xxx

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1 Journal of Fluency Disorders xxx (2010) xxx xxx Follow-up of 6 10-year-old stuttering children after Lidcombe Program : A Phase I trial Sarita Koushik a,b, Rosalee Shenker a, Mark Onslow c, a Montreal Fluency Centre, Canada b The University of Newcastle, Australia c Australian Stuttering Research Centre, The University of Sydney, Australia Received 20 August 2009; received in revised form 5 November 2009; accepted 5 November 2009 Abstract Purpose: This Phase I trial sought to establish (1) whether the Lidcombe Program is viable for school-age children, (2) whether there is any indication that it requires modification for school-age children, (3) whether effects are durable, (4) how many sessions appear to be required to significantly reduce stuttering frequency and (5) whether there is an association between follow-up period and relapse tendency. Method: Twelve children were treated, and one required an addition to the Lidcombe Program. The results for this child were excluded from group analysis, leaving a group of 6 10 year-olds. A retrospective method was used using routine pre- clinic recordings. At follow-up, all children were telephoned and audio-recorded three times at random times during the day within a 7 10-day period. Results: A blinded observer s mean percent syllables stuttered score pre- was 9.2 and 1.9 at follow-up. No association was found between follow-up period and stuttering rates. The mean syllables per minute score pre- was and at follow-up. These results were attained in a median of eight clinic visits with a range of 6 10 visits. Conclusions: Procedurally, the Lidcombe Program is viable for school-age children and parents report enjoyment in administering it. There appears to be a effect that can be attained in a reasonable number of clinical hours. These results compel continued exploration with young school-aged children in subsequent Phase II and III studies. Educational objectives: The reader will be able to: (1) summarize the status of clinical trials for stuttering school-age children, (2) describe the phases of clinical trial development, (3) evaluate outcomes the Lidcombe Program for a school-age population in terms of stuttering reduction and time, (4) evaluate the suitability of the Lidcombe Program with population of school-age stuttering children, and (5) provide an interpretation of the finding of no correlation between follow-up and post- stuttering rates Elsevier Inc. All rights reserved. Keywords: School age; Treatment; Lidcombe Program; Follow-up; Stuttering Corresponding author at: Faculty of Health Sciences, The University of Sydney, PO Box 170, Lidcombe, NSW 1825, Australia. Tel.: ; fax: addresses: sarita.koushik@gmail.com (S. Koushik), rosalee.shenker@mcgill.ca (R. Shenker), m.onslow@usyd.edu.au (M. Onslow) X/$ see front matter 2009 Elsevier Inc. All rights reserved. doi: /j.jfludis

2 2 S. Koushik et al. / Journal of Fluency Disorders xxx (2010) xxx xxx 1. Introduction It appears that stuttering is most tractable during the preschool years and that responsiveness to decreases with age, presumably because of the accompanying decrease of neural plasticity (Wohlert & Smith, 2002). On balance, available data indicate that stuttering becomes less responsive to after the preschool years (see Bothe, 2004; Bothe, Davidow, Bramlett, Franic, & Ingham, 2006; Bothe, Davidow, Bramlett, & Ingham, 2006; Ingham, 1984a, 1984b; Ingham & Cordes, 1999; Onslow, 1996; Onslow & Packman, 1997; Onslow & Packman, 1999; Prins & Ingham, 1983). The school-age period from 6 to 12 years of age might then be thought of as an important time of life for the receipt of an efficacious stuttering. Without an efficacious during the school years, the likelihood that stuttering will persist may increase with age. As a child enters the school years the demands on life naturally increase in terms of school work and social activities. Therefore, finding time to treat school-age children may be problematic as they have limited time to dedicate to approaches. Other factors to consider for school-age children are a longer history of stuttering, previous failures and the possible suffering of teasing and bullying. For these reasons efficient approaches are important for this population of children. Onslow, Jones, O Brian, Menzies, and Packman (2008) argue that methodological requirements for a clinical trial should be prospective evaluation of an entire, where speech data are collected outside the clinic with a follow-up period of at least 3 months if an effect is found. Further, Onslow et al. argue that discussion of effect sizes for different stuttering s is currently not appropriate; most stuttering trials at present are non-randomized, and their results invariably introduce biases that inflate effect sizes (Kunz & Oxman, 1998). There have been nine published clinical trials for school-age children, involving 131 school-age children. These include preliminary Phase I trials of Gradual Increase in Length and Complexity of Utterance (Ryan & Van Kirk Ryan, 1995) and regulated breathing (De Kinkelder & Boelens, 1998). There have been two Phase I trials (Ryan & Van Kirk Ryan, 1983; Ryan & Van Kirk Ryan, 1995) 1 and one Phase II trial (Lincoln, Onslow, Lewis, & Wilson, 1996) of verbal response contingent stimulation. A successful Phase II trial of EMG biofeedback has been reported, (Craig et al., 1996; Hancock et al., 1998), although there has been a failure to replicate those results (Block, Onslow, Roberts, & White, 2004). Speech restructuring involves the reduction of stuttered speech by changes in various aspects of speech production, such as reduced rate, prolonged vowels, soft articulatory contacts, and gentle vowel onsets (Packman, Onslow, & Menzies, 2000). The most popular of these programs establish stutter-free speech at a slow speech rate. Commonly, speech is then shaped to near-normal rates through programmed instruction and transferred to everyday situations. There have been three Phase I trials of this procedure with school-age children (Boberg & Kully, 1994; Budd, Madison, Itzkowitz, George, & Price, 1986; Kully & Boberg, 1991; Ryan & Van Kirk Ryan, 1995) and two Phase II trials (Craig et al., 1996; Hancock et al., 1998). No Phase III trials, incorporating randomized clinical trials evidence, have been reported. The evidence for speech restructuring is the strongest available for school-age children, with four independent replications, and no published failures to replicate. However, there may be some concerns with this style of that make it problematic for school-age children. In the first instance, this style of is based on multi-day, intensive formats that were developed for adults. These methods typically require more than 100 clinical hours (Andrews, Guitar, & Howie, 1980; Onslow, Costa, Andrews, Harrison, & Packman, 1996). It certainly is possible for such a format to be applied to school-age children with success. 2 However, such an approach may not be practical during the busy life of a school-age child. Another issue with this is the rate at which relapse occurs in adults. Estimates are between 30 and 50% in clinical trials (Boberg & Kully, 1994; Howie, Tanner, & Andrews, 1981; Martin, 1981; Perkins, 1981) and as high as 73% if relapse is defined as occurring for a significant period according to self report (Craig & Hancock, 1995). In the case of school-age children, this problem was illustrated in the Craig et al. (1996) trial. Hancock and Craig (1998) reported that around one-third of the children were stuttering in the range of 5 18% at 1 year post-. Post- relapse continued to be such a problem with this program that Craig, Hancock, and 1 The Ryan & Van Kirk Ryan (1995) contains data for GILCU, time-out (verbal response contingent stimulation) and speech restructuring. 2 In fact two of the participants in the Onslow et al. (1996) trial were of school-age, and one of them, 7-year old Participant DT, had favorable outcomes at 9 years post- (Onslow, O Brian, Packman, Rousseau, 2004).

3 S. Koushik et al. / Journal of Fluency Disorders xxx (2010) xxx xxx 3 Cobbin (2002) found it necessary to develop and test a relapse management procedure for children in this age group. The Lidcombe Program of Early Stuttering Intervention was developed for preschool-aged children. A meta-analysis of randomized clinical evidence for 34 children showed an odds ratio of 7.5 (Onslow, Jones, Menzies, O Brian, & Packman, in press). However, the has had limited trialling with school-age children. The Lincoln et al. report was based on a much earlier version of the. Verbal response contingent stimulation is non-programmed and does not involve control of stuttering with a speech pattern. As such it is potentially suitable for school-age children. The present study contributes to the development of that with a Phase I trial of this for school-age children, in order to determine whether Phase II and Phase III clinical trials are justified. Specifically, this Phase I trial seeks to establish whether (1) the Lidcombe Program is viable for school-age children, (2) whether there is any indication that it requires modification for school-age children, (3) whether effects are durable over time, (4) how many sessions appear to be required to significantly reduce stuttering frequency and (5) is there any association between follow-up period and relapse tendency. The Lidcombe Program focuses on speech outcomes (Australian Stuttering Research Centre, 2008), hence the present Phase I trial of the Lidcombe Program focuses on speech outcomes. If the Lidcombe Program appears to be associated with positive speech outcomes, then Phase II and III trials can explore whether important non-speech outcomes such as speech-related anxiety and bullying rates accompany its intended effects. Randomized Phase II and III clinical trials designs would be necessary to make such a determination, and would guide future clinical trials development for this population. 2. Method 2.1. Participants Participants were 12 children taken in order from the waiting list at the Montreal Fluency Centre, a speech and language clinic in Montreal, Canada. Participant 12 received an addition to the Lidcombe Program therefore was removed from the group analysis. The children were between the ages of 6 years 8 months and 10 years 8 months (mean = 9 years 0 months) at the start of. Ten were boys and two were girls. Stuttering was diagnosed by the presence of unambiguous stuttering (Jones et al., 2008) in the clinic sample according to the judgement of the treating speech-language pathologist (SLP) and confirmation by the parent. Exclusion criteria were pre- stuttering less than 2.0%SS as determined by the assessing SLP, first language not English, and most proficient language not English. Language proficiency was determined with the Bilingual Language History and Proficiency form (Roberts & Shenker, 2007) Assessments On the day of the assessment, the clinician measured stuttering severity in the clinic with the standard Lidcombe Program scale of 1 = no stuttering, 2 = extremely mild stuttering and 10 = extremely severe stuttering (Jones et al., 2005). The use of this scale is standard during the Lidcombe Program, and clinician severity scores are used at each clinic visit to calibrate parent severity scores. Additionally, pre- audio-recorded speech samples of the 12 children were obtained within the clinic on the day of assessment, 1 2 weeks prior to. One 10-min, pre- audio recording was obtained for each child during conversation with the clinician in the presence of the parent/s. These audio recordings were routine practice in the clinic. Follow-up assessments were conducted with random telephone calls to the children at home, in English. This method was chosen for its validity in preference to parents and children returning to the clinic for follow-up assessment. The latter method would incur potential bias from discriminated learning to the clinic of stutter-free speech, and participant selection bias of those parents willing to travel to the clinic. Additionally, unpredictable telephone calls were chosen because of their validity in preference to having parent audio- or video-recording the children in conversation. The latter method allows participants to respond to demand characteristics (Orne, 1962) cues that inform participants what behaviour is sought from researchers by self selection of speech sampling situations. The audio sampling procedure was considered suitable in light of evidence with children that audio only percent syllables stuttered (%SS) scores will not underestimate stuttering rates of post- samples (Rousseau, Onslow, Packman, & Jones, 2008). The assessment requirements for the study incurred little participation bias because pre- audio recordings

4 4 S. Koushik et al. / Journal of Fluency Disorders xxx (2010) xxx xxx were routine in the clinic. At follow-up, children needed to be available for three telephone calls in their home environment. Within a 7 10-day period, each of the children was telephoned three times, approximately every second day, at random times during the day. All follow-up speech samples were audio-recorded with an Olympus Digital Voice Recorder, using a telephone jack device. The conversations were approximately 10-min in duration and the child was asked open-ended questions in order to collect sufficient speech samples. The mean period post the conclusion of Stage 1 that the 11 children were followed up was 70 weeks with a range of weeks. On the day of the first follow-up telephone phone call, each parent was interviewed about their experience with the Lidcombe Program. The interviews were conducted by telephone before the conversations with the children and the responses were reported on a standard form and subsequently collated. The parent interviews and follow-up telephone calls were conducted by a graduate student in speech-language pathology who was blinded to the purposes of the study and who had no knowledge of the parents and children. Two of the children had English as their dominant language with French as a second language introduced at 4 years or older. At the time of, these children had very limited exposure to French and thus were categorized as English dominant. Three children were bilingual English with French, Hebrew or Italian introduced simultaneously from birth. The predominant language spoken by these three children was English. The remaining six children were introduced to a second language at 4 years or older with English as their predominant language and second language of Italian, Greek or Portuguese. Parents reported stuttering in all languages spoken. Of these 11 children, seven did not present with any other speech or language concerns, one presented with a receptive and expressive language disorder, one with an articulation disorder and one with an expressive language disorder and diagnosed attention deficit hyperactivity disorder. All children received in English and verbal contingencies applied by parents beyond the clinic were in English. For those children presenting with other speech or language concerns, remediation of those concerns followed for stuttering. Details of the children are presented in Table The The was the Lidcombe Program of Early Stuttering Intervention (Jones et al., 2005; Onslow, Packman, & Harrison, 2003). The Lidcombe Program is a behavioral developed for preschool children who stutter. It involves verbal response contingent stimulation and is administered by parents. The Lidcombe Program incorporates weekly visits to the speech clinic by the child and parent, during which the SLP trains the parent to present three verbal contingencies for the child s stutter-free speech, and two verbal contingencies for unambiguous stuttering. The verbal contingencies for stutter-free speech are acknowledgment, praise and request for self-evaluation. The contingencies for unambiguous stuttering are acknowledgement and request for self-correction. Initially, the parent presents these verbal contingencies in short, structured conversations each day that are designed to maximize the occurrence of contingencies for stutter-free speech. The parent then administers the contingencies in everyday conversations. Clinician speech measures in the clinic and parent speech measures beyond the clinic are used to guide the clinical process. Criteria for ending Stage 1 of the and beginning Stage 2 (maintenance) are (1) Percent syllables stuttered (%SS) less than 1.0 within the clinic, and (2) severity ratings (SRs) scores for the previous week of 1 or 2, with at least four of these being 1 (Australian Stuttering Research Centre, 2008, p. 8). For all children, the Lidcombe Program was conducted in the child s strongest language, which was English. Verbal contingencies applied beyond the clinic were also provided in English. The criteria for ending Stage 1 of and beginning Stage 2 were more stringent than for manualized for preschool children (see above). Since the clinical response of these children was much quicker than for preschool children (see below), it was felt that imposing more stringent criteria for entry into Stage 2 would create a hedge against relapse during the early weeks of Stage 2. In the present study, the criteria for entering Stage 2 were (1) %SS less than 1.0 within the clinic, and (2) SR scores for the previous week of 1 each day for either three consecutive visits or two consecutive clinic visits spanning 3 weeks during which there was an intervening non-attendance at the clinic (3-week period) Outcome measures The primary outcome measure was percent syllables stuttered (%SS). A secondary speech outcome was syllables per minute (SPM). A non-speech secondary outcome was the number of clinic sessions to reach Stage 2. The latter

5 S. Koushik et al. / Journal of Fluency Disorders xxx (2010) xxx xxx 5 Table 1 Details of the participants. Stuttering scores in the last two columns are from the blinded, independent observer. Participant Gender Previous Details of previous Subsequent Details of subsequent Language background Other speech/language concerns 1 Boy Yes Articulation No L1 = E; L2 = I; L3 = F 2 Boy Yes 4 6 stuttering sessions at No L1 = H; L2 = E; L3 = F 3 years of age 3 Girl No No L1 = E; L2 = F 4 Boy Yes 3 4 stuttering sessions, articulation No L1 = E; L2 = I; L3 = F 5 Girl No No L1 = E; L2 = F 6 Boy Yes Stuttering at school which involved exercises for breathing No L1 = E; L2 = I; L3 = F 7 Boy No No L1 = E; L2 = F Expressive language disorder 8 Boy Yes Stuttering at school which involved breathing and pausing No L1 = F; L2 = E; L3 = P 9 Boy No Yes 1 follow-up session at Children s hospital L1 = E; L2 = F 10 Boy Yes Articulation No L1 = E; L2 = F; L3 = I 11 Boy No No L1 = E; L2 = G; L3 = F 12 Boy No No L1 = E; L2 = F ADHD/expressive language disorder Articulation disorder Receptive and expressive language disorder L1, first language; L2, second language; L3, third language. Language: E, English; F, French; G, Greek; H, Hebrew; I, Italian; P, Portuguese. Note: Participant 11 entered Stage 2 with speech criteria more liberal than the study criteria. Participant 12 received a speech-restructuring additive to and was not included in the group report. measure is important in terms of cost efficiency of delivery, and benchmarks are available for the Lidcombe Program. The collective findings of previous clinical trials (Jones et al., 2005; Onslow, Andrews, & Lincoln, 1994; Rousseau, Packman, Onslow, Harrison, & Jones, 2007) and large cohort recovery plot studies (Jones, Onslow, Harrison, & Packman, 2000; Kingston, Huber, Onslow, Jones, & Packman, 2003) convey that a median of around 12 sessions are required for preschool children to be at the requisite low stuttering levels for entry to Stage 2 of (maintenance). With the imposition of more rigorous criteria in the recent version of the manual (Australian Stuttering Research Centre, 2008), Rousseau et al. reported a median of 16 clinic visits to attain Stage 2. Consistent with the methodological recommendations of Bothe, Davidow, Bramlett, Franic, et al. (2006) and Bothe, Davidow, Bramlett, and Ingham (2006), speech naturalness was not included as an outcome because the does not involve the use of a novel speech pattern. Prior to therapy, there was no instruction for the children to use speech restructuring nor were they asked to change the way they spoke throughout the. A total of 44 speech samples (11 participants 4 assessments) were obtained. The follow-up samples were pooled to provide 11 samples, each of approximately 30 min duration. The mean number of syllables in the pooled follow-up samples was 1427 syllables (SD = 218, range ). The mean number of syllables in the pre- samples was 439 (SD = 72, range ). All speech samples were transferred to a Windows XP operating system

6 6 S. Koushik et al. / Journal of Fluency Disorders xxx (2010) xxx xxx Table 2 Details of follow-up samples. Participant Gender Age at onset of Number of weeks to Stage 2 Age at follow-up Number of weeks at follow-up Pre- %SS a Severity rating at assessment Mean %SS at follow-up weeks 1 Boy 10;3 6 10; b Boy 9;5 7 9; Girl 6;9 8 7; Boy 10; ; Girl 8;9 6 12; Boy 8; ; Boy 7;4 10 8; Boy 10;3 9 11; Boy 9;4 6 11; Boy 9;8 8 12; Boy 6;8 8 7; Boy 10;8 7 14; a Severity rating = a scale from 1 to 10, where 1 = no stuttering and 10 = extreme stuttering for that child. For this measure the clinician and parent jointly rated the severity of stuttering on the day of the assessment. b Exclusion criteria were pre- stuttering less than 2.0%SS as determined by the assessing SLP. However, the blinded observer s score for this child differed slightly from the assessing clinician. and stored in a media audio format. The observer of all speech samples in the study was an independent, New Zealand based SLP who was blinded to the purposes of the study. All speech samples were evaluated for %SS. A button-press counting and timing device (True Talk) was used to measure %SS and SPM for each sample while listening to the sample through headphones. The speech recordings were presented to the blinded observer, de-identified and in random order. The observer was not instructed to base stuttering counts on behavioral criteria of any kind. Instead, consistent with measurement procedures of the Lidcombe Program (Onslow et al., 2003), the observer was instructed to use a perceptual procedure and to count as stuttering any speech events that were considered unambiguously to be so. The observer was experienced with the Lidcombe Program and consequently experienced with this measurement method. The measures obtained by the blinded observer are reported as outcomes for the trial and are presented in Table 2 (Fig. 1). 3. Results 3.1. Clinical progress Only one child (Participant 12) required a supplement to the Lidcombe Program. This boy received the addition of a speech-restructuring component in addition to the Lidcombe Program. His results were excluded from the group results presented below for the 11 children who received only the Lidcombe Program. Of the 11 participants in total, Fig. 1. Pre- and follow-up %SS scores for the individual children by a blinded observer. Note: Participant 11 entered Stage 2 with speech criteria more liberal than the study criteria.

7 S. Koushik et al. / Journal of Fluency Disorders xxx (2010) xxx xxx 7 eight had completed Stage 2 at the time of the follow-up telephone calls. Three participants (Participant 1, 2 and 9) had not completed Stage 2 at that time but all subsequently did so Outcomes Primary outcome For the 11 school-age children who received the Lidcombe Program, the blinded observer s mean %SS score pre- was 9.2 (SD = 7.8) and 1.9 (SD = 1.3) at follow-up (t[10] = 5.77, p =.0002). 3 Six months after the original measurements, three pre- and three follow-up recordings were randomly selected and re-represented to the blinded observer to determine intra-observer reliability. The tapes ranged in initial %SS scores of the blinded observer from 16.1 to 0. All second %SS scores differed from the first by 1.0%SS or less, with a correlation of.997 (p <.001). Despite large stuttering reductions at follow-up, three of the children s follow-up stuttering rates were greater than 3.0%SS (see Table 2). For inter-observer reliability purposes, these data were compared to those obtained using the same methods by the treating SLP in Canada. The unblinded treating clinician scored lower than the blinded observer, with mean %SS scores pre- of 7.2 (SD = 5.1) and 0.9 (SD = 0.5). The difference between the two observers %SS scores pre- was not significant (t[10] = 1.04, p =.33). Difference between observers follow-up %SS scores was significant (t[10] = 5.31, p =.0003). This result was predictable considering that the treating clinician was extremely familiar with the children. However, the %SS scores of the blinded and clinician observers correlated highly at.91 (p <.001) Secondary outcomes These results were attained in a median of eight clinic visits (Range 6 10 visits). For the 11 school-age children who received the Lidcombe Program, the blinded observer s mean SPM pre- score was (SD = 22.7) and (SD = 20.5) at follow-up (t[10] = 3.19, p =.0097). The SPM scores of the blinded and clinician observers correlated significantly at.58 (p <.05). This result is consistent with improved verbal output associated with stuttering reduction. It also indicates that stuttering reductions were not attained at the cost of reduced speech rate Correlation between outcomes and follow-up period As with any retrospective study, there was a wide range of follow-up periods as noted in Table 1. Pearson correlations were calculated for %SS scores at follow-up and number of weeks to follow-up in order to assess any tendencies for relapse during the post- period. A nonsignificant correlation of.20 (p =.51) shows that the follow-up period explains only.04 of the variance in follow-up %SS scores. This indicates the absence of a relationship between relapse and duration of time post- with this group of children Individual cases One of the two children in the study with moderate language disorders (Participant 11) was admitted to Stage 2 with speech performance close to, but not below, the criteria as stated above. This was the only child in the study with a receptive language disorder, however this did not appear to impede his understanding of verbal contingencies. However, receptive and expressive language difficulties seemed to be hindering his progress in attaining the study speech criteria. The clinician noted that when this child was formulating thoughts and ideas to explain something difficult, he tended to stutter more when he was unsure of how to formulate his utterances. Stuttering occurred when he had difficulty with vocabulary, sentence structure or the sequence of ideas. Further, he stuttered more on conjunctions that preceded new ideas. In linguistically undemanding conversational exchanges between this child and the clinician, %SS in the clinic was typically below 1.0. The parents of this child consistently assigned SRs of 1 and 2 for a period of three clinical sessions, without further progress. It was decided that this child would be admitted to Stage 2 with %SS measures in the clinic below 2.0 and a mean SR each week of 2 or below. During Stage 2, attempts were made to maintain these levels while he received language therapy. If the parent/s reported SRs higher than 2, they were asked to 3 Because of small sample size, this and other paired t-tests in this report were log transformed prior to analysis, as recommended by Jones, Onslow, Packman, and Gebski (2006).

8 8 S. Koushik et al. / Journal of Fluency Disorders xxx (2010) xxx xxx Table 3 Parent satisfaction with the Lidcombe Program. Parent questionnaire %yes %no Since your last visit to the clinic has your child s fluency worsened? 20% 80% Overall how would you rate child s speech severity in terms of severity ratings (SRs), at this time? SR 1 1 parent 10% SR 2 6 parents 60% SR 3 3 parents 30% SR 4 0 parents 0% Are you continuing to give feedback for child s speech? (i.e. positive reinforcement 80% 20% for fluency, request for correction for stuttering) Besides stuttering, do you have other speech and language concerns for your child? 20% 80% Has your child been seen by another SLP for stuttering since leaving our clinic? 10% 90% Did you enjoy participating in the LP? 100% LP factors that were difficult? finding 10 min a day for therapy 60% 40% giving feedback to your child 30% 70% increase their verbal contingencies in both 10-min structured and unstructured conversations until the SRs decreased to 2 or below. Participant 11, who received language, was admitted to Stage 2 in eight clinic visits, with the above study criteria. The remaining 10 participants attained Stage 2 in a median of 7.5 clinic visits (mean = 7.6, range = 6 10 clinic visits). For Participant 4, the %SS measures at follow-up were higher than pre- conversation in the clinic, suggesting no effect. With this child, Stage 2 goals for maintenance of stutter-free speech were not being met. During the parent interview, a number of compliance issues emerged. The parent was unique in providing verbal contingences only for stuttered speech but no verbal contingencies acknowledgement, praise and request for self-evaluation for stutter-free speech. This parent was one of several parents (see below) who reported difficulty in finding a short time each day for in structured conversations Parent interviews The parents of 10 of the school-age children in this study were interviewed about their satisfaction with the Lidcombe Program. The remaining 2 parents were not available for the interview. Using the Lidcombe Program SR scale (1 = no stuttering, 2 = extremely mild stuttering, 10 = extremely severe stuttering), seven (70%) parents assigned a score of 1 or 2 to their child s speech, while three (30%) parents assigned scores of 3. No parents scored the child s SR at 4 or greater. Eight parents (80%) reported that the child s stuttering had not worsened since their last clinical visit and two (20%) reported a slight increase. Eight (80%) parents reported that they continued to provide occasional verbal contingencies to their children for stutter-free and stuttered speech. All parents indicated that they enjoyed participating in the Lidcombe Program, however six (60%) reported that they found it difficult to find time to conduct in structured conversations each day, mainly because of busy home schedules. Table 3 summarizes the parent questionnaire responses. 4. Discussion Given that stuttering is more tractable during childhood, it is clear that efficacious stuttering for school-age children is of great importance. Verbal response contingent stimulation procedures such as the Lidcombe Program used in this study are not complicated by programmed instruction or the use of a novel speech pattern. Generally, this Phase I trial presented positive answers to the questions driving the research. Procedurally, the Lidcombe Program is viable for school-age children and parents report enjoyment in administering it. In all but one of the 12 children studied, it required no modification to the manualized procedures for school-age children. There is some reason to believe that

9 S. Koushik et al. / Journal of Fluency Disorders xxx (2010) xxx xxx 9 over a period of time, there is a stuttering reduction effect that can be attained in a reasonable number of clinical hours. No association was found between follow-up period and stuttering rates, suggesting the durability of any effects. These results compel continued exploration of the Lidcombe Program with young school-aged children in subsequent Phase II and III clinical trials. For the 11 school-age children, the blinded observer s mean %SS scores pre- was 9.2 and 1.8 at follow-up. These results were obtained in a median of eight clinic visits. Four of those children at follow-up had %SS scores below 1.0, four had %SS scores below 3.0 and three had %SS scores below 4.0. The 11 children received by a clinician in a different country than that in which the Lidcombe Program was originally developed. Therefore, this report independently substantiates the Lincoln et al. (1996) findings of the benefits of a much earlier version of the Lidcombe Program with this age group. The program is worthy of continued clinical trials development with this age group. Although four of the 11 participants maintained an average %SS below 1.0% at follow-up, seven others did not achieve this criterion which suggests that there is more variability in Stage 2 outcomes for the school-age population compared to preschool children (Jones et al., 2005). This variability is comparable with the findings obtained for schoolage children from Lincoln et al. (1996). This raises questions about what factors might contribute to this variability in the school-age population. Of course, these results pertain to speech improvements. Should these results be replicated with prospective, randomized clinical trial designs, it will be of interest subsequently to determine whether any non-speech improvements can also occur as expediently. There are clinical trials data, for example, that provide some indication of the clinical time required for efficacious management of speech-related social anxiety (Menzies et al., 2008). It is likely that such anxiety is present with the age group studied here. In which case, it may be that efficacious anxiety management with the present age group can be an expedient matter. In the case of Participant 12 the treating clinician judged that progress was not satisfactory with the Lidcombe Program alone and supplemented it with traditional speech-restructuring targets. This decision was made because the was not suitable for the child s parent. The parent found it difficult to give the verbal contingences. Additionally, this parent reported only providing occasional contingencies for stuttered speech. Therefore, the clinician introduced speech-restructuring components so that Participant 12 would not need to rely completely on parental verbal contingencies for the control of his stuttering. With the aid of the speech-restructuring supplement, Participant 12 did reach Stage 2 in seven clinic visits (see Table 2). The blinded observer s %SS score pre- was 8.3 and 2.5 at follow-up. For this child, the combination of the two styles did not result in a superior outcome to the other participants in the study. One of the two children with language disorders (Participant 11) who received the Lidcombe Program needed to enter Stage 2 with more liberal criteria as judged by the treating clinician. The reason for this was because language problems were felt to be a barrier for attaining the study speech criteria. Nonetheless, this child appeared to benefit from the up until the time of follow-up. However, this raises an issue for future research about the characteristics of school-age children for whom the Lidcombe Program is suitable, and the factors such as the presence or absence of language disorders that may affect outcomes for children with these profiles. One of the encouraging findings for the children in this study is the number of sessions required. If 16 clinic visits is considered a reasonable benchmark for the time to attain speech criteria for admission to Stage 2 (see Section 1), the present report of half that number, with a median of eight, is encouraging. One reason it may have occurred is because of the enhanced cognitive functioning of school-age children and their increased capacity to selfdirect their. A meta-analysis of available data (Kingston et al., 2003) suggest that may be shorter for older children in the preschool age range, and the present results may represent an extension of that effect into the school-age years. However, the present finding is based on a small cohort of children and requires replication. The present results of a verbal response contingent program for stuttering school-age children are encouraging. However, the study was preliminary and retrospective, and hence it is likely to contain positive bias associated with participant selection. Another limitation of the present report is that it compared recordings in the clinic pre with telephone recordings at follow-up. However, as noted in Section 2 (see Section 2.2), this was a less bias-prone procedure than having the children return to the clinic. Further, as is the case with the majority of clinical trials of stuttering, there was a risk of underestimating follow-up stuttering rates with audio observations. The present study used telephone post- speech samples. However, at least for non-telephone audio samples, the risk of error appears minimal (Rousseau et al., 2007). The above limitations aside, the study was of an age group not renown

10 10 S. Koushik et al. / Journal of Fluency Disorders xxx (2010) xxx xxx for natural recovery, hence the occurrence of that event with the children would not have been a likely source of bias. Overall, the findings justify the conduct of Phase II and III clinical trials to establish effects of the Lidcombe Program for school-age children. It may well prove to be a valuable contribution to stuttering that is greatly needed for this age group of children who stutter. CONTINUING EDUCATION Follow-up of 6 10-year-old stuttering children after Lidcombe Program : A Phase I trial QUESTIONS 1. According to Onslow et al. (in press), which of the following is not a clinical trial of a stuttering : (a) A fundamental interpretable unit of efficacy (b) At least one pre- and one follow-up outcome measure (c) An attempt to determine outcome with retrospective data (d) An attempt to determine outcome with prospective data 2. What phase of clinical trials is known as the gold-standard evidence for efficacy? (a) Phase I (b) Phase II (c) Phase III (d) All of the above 3. The Lidcombe Program: (a) Is a behavioural approach developed for school-age children who stutter (b) Is administered only by a speech-language pathologist (c) Involves verbal response contingent stimulation (d) All of the above 4. Treatments for school-age children are needed urgently (a) Because there are none (b) Because there has been only one clinical trial (c) Because they are known to be bullied during the school years because of stuttering (d) None of the above 5. This study found (a) Clinical trials evidence in favour of the Lidcombe Program for school-age children (b) Evidence to warrant clinical trials of the Lidcombe Program with that age group (c) No suggestion of a effect at all (d) None of the above Acknowledgments This project was supported by Program Grant from the National Health and Medical Research Council of Australia (NHMRC). The project was supported in part by a student research grant from the McGill University Faculty of Medicine and the Alvin Segal Family Foundation. We would like to thank the parents and children who participated in this project. Special thanks to Anna Hearn, Elisabeth Harrison, Ann Packman and Sue O Brian for their support with this project. Very special thanks to Ben Adaman for collection of the telephone samples and subsequent assistance in preparation of the document for publication. References Andrews, G., Guitar, B., & Howie, P. (1980). Meta-analysis of the effects of stuttering. Journal of Speech and Hearing Disorders, 45,

11 S. Koushik et al. / Journal of Fluency Disorders xxx (2010) xxx xxx 11 Australian Stuttering Research Centre. (2008). Manual for the Lidcombe Program of early stuttering intervention. Retrieved August 7, 2008, from Manual English April 2008.pdf. Block, S., Onslow, M., Roberts, R., & White, S. (2004). Control of stuttering with EMG feedback. Advances in Speech Language Pathology, 6(2), Boberg, E., & Kully, D. (1994). Long-term results of an intensive program for adults and adolescents who stutter. Journal of Speech & Hearing Research, 37(5), Bothe, A. K. (2004). Evidence-based of stuttering: Empirical bases and clinical applications. Mahwah, NJ: Lawrence Erlbaum Associates. Bothe, A. K., Davidow, J. H., Bramlett, R. E., Franic, D. M., & Ingham, R. J. (2006). Stuttering research II. Systematic review incorporating trial quality assessment of pharmacological approaches. American Journal of Speech-Language Pathology, 15(4), Bothe, A. K., Davidow, J. H., Bramlett, R. E., & Ingham, R. J. (2006). Stuttering research I. Systematic review incorporating trial quality assessment of behavioral, cognitive, and related approaches. American Journal of Speech-Language Pathology, 15(4), Budd, K. S., Madison, L. S., Itzkowitz, J. S., George, C. H., & Price, H. A. (1986). Parents and therapists as allies in behavioral of children s stuttering. Behavior Therapy, 17(5), Craig, A., Hancock, K., Chang, E., McCready, C., Shepley, A., McCaul, A., et al. (1996). A controlled clinical trial for stuttering in persons aged 9 to 14 years. Journal of Speech & Hearing Research, 39(4), Craig, A., Hancock, K., & Cobbin, D. (2002). Managing adolescents who relapse following for stuttering. Asia Pacific Journal of Speech, Language & Hearing, 7(2), Craig, A. R., & Hancock,. (1995). Self-reported factors related to relapse following for stuttering. Australian Journal of Human Communication Disorders, 23(1), De Kinkelder, M., & Boelens, H. (1998). Habit-reversal for children s stuttering: Assessment in three settings. Journal of Behavior Therapy & Experimental Psychiatry, 29(3), Hancock, K., & Craig, A. (1998). Predictors of stuttering relapse one year following for children aged 9 to 14 years. Journal of Fluency Disorders, 23(1), Hancock, K., Craig, A., McCready, C., McCaul, A., Costello, D., Campbell, K., et al. (1998). Two- to six-year controlled-trial stuttering outcomes for children and adolescents. Journal of Speech Language and Hearing Research, 41(6), Howie, P. M., Tanner, S., & Andrews, G. (1981). Short-term and long-term outcome in an intensive program for adult stutterers. Journal of Speech and Hearing Disorders, 46, Ingham, R. (1984a). Techniques for maintaining fluency. In W. Perkins (Ed.), Current therapy of communication disorders: Stuttering disorders (pp ). New York: Thieme-Stratton. Ingham, R. (1984b). Stuttering and behavior therapy: Current status and experimental foundations. San Diego, CA: College-Hill Press. Ingham, R. J., & Cordes, A. K. (1999). On watching a discipline shoot itself in the foot: Some observations on current trends in stuttering research. In N. B. Ratner, & C. E. Healey (Eds.), Stuttering research and practice: Bridging the gap (pp ). Mahwah, NJ: Lawrence Erlbaum Associates. Jones, M., Hearne, A., Onslow, M., Packman, A., Ormond, T., Williams, S., et al. (2008). Extended follow up of a randomised controlled trial of the Lidcombe Program of early stuttering intervention. International Journal of Language & Communication Disorders, 43, Jones, M., Onslow, M., Harrison, E., & Packman, A. (2000). Treating stuttering in young children: Predicting time in the Lidcombe Program. Journal of Speech Language and Hearing Research, 43(6), Jones, M., Onslow, M., Packman, A., & Gebski, V. (2006). Guidelines for statistical analysis of percentage of syllables stuttered data. Journal of Speech, Language and Hearing Research, 49, Jones, M., Onslow, M., Packman, A., Williams, S., Ormond, T., Schwarz, I., et al. (2005). Randomised controlled trial of the Lidcombe programme of early stuttering intervention. British Medical Journal, 331(7518), Kingston, M., Huber, A., Onslow, M., Jones, M., & Packman, A. (2003). Predicting time with the Lidcombe Program: Replication and meta-analysis. International Journal of Language & Communication Disorders, 38(2), Kully, D., & Boberg, E. (1991). Therapy for school-age children. Seminars in Speech and Language, 12, Kunz, R., & Oxman, A. D. (1998). The unpredictability paradox: review of empirical comparisons of randomized and non-randomized clinical trials. British Medical Journal, 317, Lincoln, M., Onslow, M., Lewis, C., & Wilson, L. (1996). A clinical trial of an operant for school-age children who stutter. American Journal of Speech-Language Pathology, 5(2), Martin, R. (1981). Introduction and perspective: Review of published research. In E. Boberg (Ed.), Maintenance of fluency: Proceedings of the Banff Conference. New York: Elsevier. Menzies, R., O Brian, S., Onslow, M., Packman, A., St Clare, T., & Block, S. (2008). An experimental clinical trial of a cognitive behavior therapy package for chronic stuttering. Journal of Speech, Language and Hearing Research, 51, Onslow, M. (1996). Behavioral management of stuttering. San Diego, CA: Singular Publishing Group. Onslow, M., Andrews, C., & Lincoln, M. (1994). A control-experimental trial of an operant for early stuttering. Journal of Speech & Hearing Research, 37(6), Onslow, M., Costa, L., Andrews, C., Harrison, E., & Packman, A. (1996). Speech outcomes of a prolonged-speech for stuttering. Journal of Speech & Hearing Research, 39(4), Onslow, M., Jones, M., Menzies, R., O Brian, S., & Packman, A. (in press). Stuttering. In P. Sturmey & M. Hersen (Eds.), Handbook of evidence-based practice in clinical psychology. Hoboken, NJ: Wiley. Onslow, M., Jones, M., O Brian, S., Menzies, R., & Packman, A. (2008). Defining, identifying, and evaluating clinical trials of stuttering s: A tutorial for clinicians. American Journal of Speech-Language Pathology, 17,

12 12 S. Koushik et al. / Journal of Fluency Disorders xxx (2010) xxx xxx Onslow, M., O Brian, S., Packman, A., & Rousseau, I. (2004). Long term follow up of speech outcomes for a prolonged-speech for stuttering: The effects of paradox on stuttering research. In A. K. Bothe (Ed.), Evidence-based of stuttering: Empirical issues and clinical implications.. Mahwah, NJ: Lawrence Erlbaum Associates. Onslow, M., & Packman, A. (1997). Issues in of early stuttering. Journal of Fluency Disorders, 22(2), Onslow, M., & Packman, A. (Eds.). (1999). The handbook of early stuttering intervention. San Diego, CA: Singular Publishing Group. Onslow, M., Packman, A., & Harrison, E. (Eds.). (2003). The Lidcombe program of early stuttering intervention: A clinician s guide. Austin, TX: Pro-Ed. Orne, M. (1962). On the social psychology of the psychological experiment: With particular reference to demand characteristics and their implications. American Psychologist, 17, Packman, A., Onslow, M., & Menzies, R. (2000). Novel speech patterns and the of stuttering. Disability & Rehabilitation, 22(1 2), Perkins, W. (1981). Implications of scientific research for the of stuttering: A lecture. Journal of Fluency Disorders, 6, Prins, D., & Ingham, R. J. (1983). Treatment of stuttering in early childhood: Methods and issues. San Diego, CA: College-Hill Press. Roberts, P. M., & Shenker, R. C. (2007). Assessment and of stuttering in bilingual speakers. In E. G. Conture, & R. F. Curlee (Eds.), Stuttering and related disorders of fluency (3rd ed., pp ). New York: Thieme. Rousseau, I., Onslow, M., Packman, A., & Jones, M. (2008). Comparisons of audio and audio visual measures of stuttering frequency and severity in preschool age children. American Journal of Speech-Language Pathology, 17, Rousseau, I., Packman, A., Onslow, M., Harrison, L., & Jones, M. (2007). An investigation of language and phonological development and the responsiveness of preschool age children to the Lidcombe Program. Journal of Communication Disorders, 40(5), Ryan, B. P., & Van Kirk Ryan, B. (1995). Programmed stuttering for children: Comparison of two establishment programs through transfer, maintenance, and follow-up. Journal of Speech & Hearing Research, 38(1), Ryan, B. P., & Van Kirk Ryan, B. (1983). Programmed stuttering therapy for children: Comparison of four establishment programs. Journal of Fluency Disorders, 8, Wohlert, A. B., & Smith, A. (2002). Developmental change in variability of lip muscle activity in speech. Journal of Speech, Language and Hearing Research, 45, Sarita Koushik has a Master s degree in speech-language pathology from the University of Alberta, Canada. She has specialized in stuttering for the past 8 years with a particular focus on preschool and school-age children. Currently, Sarita is pursuing her doctoral degree at the University of Newcastle, Australia in preschool stuttering. Rosalee Shenker is Founder and Executive Director of the Montreal Fluency Centre and adjunct Professor at McGill University, Department of Communication Sciences and Disorders. She has pursued her interests in evidence-based of stuttering with publications and presentations that focus on aspects of bilingualism and linguistic proficiency in children who stutter. Mark Onslow is the Director of the Australian Stuttering Research Centre. He is a Principal Research Fellow of the National Health and Medical Research Council of Australia, an Adjunct Professor at the University of Canterbury, New Zealand, and an Honorary Professor at the University of Queensland, Australia.

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